Product Details

SNP ID

rs1129208

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:18592314 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTCCTGCAGTTCCAGACACCTCCC[A/C]CAATAAAGAGCTCCTCCTCTGTAGC

Phenotype

MIM: 604237

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

C19orf60 PubMed Links

Additional Information

For this assay, SNP(s) [rs112466988] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

C19orf60

Gene Name

chromosome 19 open reading frame 60

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100418.1	778	UTR 3			NP_001093888.1
NM_001100419.1	778	UTR 3			NP_001093889.1
XM_005259977.1	778	UTR 3			XP_005260034.1

Gene

CRLF1

Gene Name

cytokine receptor like factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004750.4	778	Intron			NP_004741.1
XM_011528422.2	778	Intron			XP_011526724.1
XM_011528423.2	778	Intron			XP_011526725.1
XM_011528424.2	778	Intron			XP_011526726.1

View Full Product Details